Canonical Allele Identifier: CA380690962

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382047G>T (hg19) ; chr11:g.57614574G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614574G>T , CM000673.2:g.57614574G>T	GRCh38
NC_000011.9:g.57382047G>T , CM000673.1:g.57382047G>T	GRCh37
NC_000011.8:g.57138623G>T	NCBI36
NG_009625.1:g.22021G>T , LRG_105:g.22021G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1496G>T MANE Select	ENSP00000278407.4:p.Arg499Met
ENST00000528996.2:c.*393G>T	ENSP00000431226.2:n.*393G>T
ENST00000531605.2:c.*1272G>T	ENSP00000503752.1:n.*1272G>T
ENST00000619430.2:c.1292G>T	ENSP00000478572.2:p.Arg431Met
ENST00000676670.1:c.1496G>T	ENSP00000504807.1:p.Arg499Met
ENST00000676741.1:n.2578G>T
ENST00000677624.1:c.*916G>T	ENSP00000503979.1:n.*916G>T
ENST00000677625.1:c.1442G>T	ENSP00000502857.1:p.Arg481Met
ENST00000677856.1:n.1749G>T
ENST00000677915.1:c.*393G>T	ENSP00000503118.1:n.*393G>T
ENST00000678533.1:c.*1050G>T	ENSP00000503873.1:n.*1050G>T
ENST00000678592.1:c.*436G>T	ENSP00000504424.1:n.*436G>T
ENST00000278407.8:c.1496G>T	ENSP00000278407.4:p.Arg499Met
ENST00000340687.10:c.1385G>T	ENSP00000341861.6:p.Arg462Met
ENST00000378323.8:c.1511G>T	ENSP00000367574.4:p.Arg504Met
ENST00000378324.6:c.1340G>T	ENSP00000367575.2:p.Arg447Met
ENST00000403558.1:c.1625G>T	ENSP00000384420.1:p.Arg542Met
ENST00000528996.1:c.697G>T	ENSP00000431226.1:n.697G>T
ENST00000531133.5:c.997G>T	ENSP00000435431.1:n.997G>T
ENST00000531797.5:c.*521G>T	ENSP00000432554.1:n.*521G>T
ENST00000619430.1:c.627G>T	ENSP00000478572.1:n.627G>T
NM_000062.2:c.1496G>T , LRG_105t1:c.1496G>T	NP_000053.2:p.Arg499Met
NM_001032295.1:c.1496G>T	NP_001027466.1:p.Arg499Met
NM_000062.3:c.1496G>T MANE Select	NP_000053.2:p.Arg499Met
NM_001032295.2:c.1496G>T	NP_001027466.1:p.Arg499Met